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Create atlas/splitmerge Module (#1756)
* Add atlas/splitmerge module * Finish the tests for atlas/splitmerge * Prettier * Update modules/atlas/splitmerge/meta.yml Co-authored-by: James A. Fellows Yates <jfy133@gmail.com> * Remove curly brackets from meta.yml parameters For single-file outputs, as reviewed * Lintung: Remove trailing white-space Co-authored-by: James A. Fellows Yates <jfy133@gmail.com>
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36
modules/atlas/splitmerge/main.nf
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36
modules/atlas/splitmerge/main.nf
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process ATLAS_SPLITMERGE {
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tag "$meta.id"
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label 'process_low'
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conda (params.enable_conda ? "bioconda::atlas=0.9.9" : null)
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container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
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'https://depot.galaxyproject.org/singularity/atlas:0.9.9--h082e891_0':
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'quay.io/biocontainers/atlas:0.9.9--h082e891_0' }"
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input:
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tuple val(meta), path(bam), path(bai), path(read_group_settings), path(blacklist)
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output:
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tuple val(meta), path("*_mergedReads.bam"), path("*.txt.gz"), emit: data
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path "versions.yml", emit: versions
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when:
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task.ext.when == null || task.ext.when
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script:
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def optional = blacklist ? 'blacklist=${blacklist}' : ''
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def args = task.ext.args ?: ''
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def prefix = task.ext.prefix ?: "${meta.id}"
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"""
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atlas \\
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task=splitMerge bam=${bam} \\
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readGroupSettings=${read_group_settings}\\
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$optional \\
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$args
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cat <<-END_VERSIONS > versions.yml
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"${task.process}":
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atlas: \$((atlas 2>&1) | grep Atlas | head -n 1 | sed -e 's/^[ \t]*Atlas //')
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END_VERSIONS
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"""
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}
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70
modules/atlas/splitmerge/meta.yml
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70
modules/atlas/splitmerge/meta.yml
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name: "atlas_splitmerge"
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description: split single end read groups by length and merge paired end reads
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keywords:
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- split
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- merge
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- bam
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- read group
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tools:
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- "atlas":
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description: "ATLAS, a suite of methods to accurately genotype and estimate genetic diversity"
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homepage: "https://bitbucket.org/wegmannlab/atlas/wiki/Home"
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documentation: "https://bitbucket.org/wegmannlab/atlas/wiki/Home"
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tool_dev_url: "https://bitbucket.org/wegmannlab/atlas"
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doi: "10.1101/105346"
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licence: "['GPL v3']"
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input:
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- meta:
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type: map
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description: |
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Groovy Map containing sample information
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e.g. [ id:'test', single_end:false ]
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- bam:
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type: file
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description: Single input BAM file.
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pattern: "*.bam"
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- bai:
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type: file
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description: The BAI file for the input BAM file
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pattern: "*.bai"
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- read_group_setting:
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type: file
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description: |
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TXT file containing the split and merge settings for
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each readgroup. Each line consist of one readgroup,
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single/double identifier and the maximum cycle number
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of the sequencer. e.g. "RG1 single 100"
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pattern: "*.txt"
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- blacklist:
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type: file
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description: |
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blacklist.txt (optional), A txt file with blacklisted read names
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that should be ignored and just written to file, each on a new line
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pattern: "*.txt"
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output:
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- meta:
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type: map
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description: |
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Groovy Map containing sample information
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e.g. [ id:'test', single_end:false ]
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- versions:
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type: file
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description: File containing software versions
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pattern: "versions.yml"
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- bam:
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type: file
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description: A BAM file with suffix_mergedReads.bam
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pattern: "*_mergedReads.bam"
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- filelist:
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type: file
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description: A file listing all reads that were filtered out in the merging process with suffix_ignoredReads.txt.gz
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pattern: "*.txt.gz"
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authors:
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- "@merszym"
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@ -78,6 +78,10 @@ ataqv/ataqv:
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- modules/ataqv/ataqv/**
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- tests/modules/ataqv/ataqv/**
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atlas/splitmerge:
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- modules/atlas/splitmerge/**
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- tests/modules/atlas/splitmerge/**
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bakta:
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- modules/bakta/**
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- tests/modules/bakta/**
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@ -235,7 +235,9 @@ params {
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mitochon_standin_recalibrated_sorted_bam = "${test_data_dir}/genomics/homo_sapiens/illumina/bam/mitochon_standin.recalibrated.sorted.bam"
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mitochon_standin_recalibrated_sorted_bam_bai = "${test_data_dir}/genomics/homo_sapiens/illumina/bam/mitochon_standin.recalibrated.sorted.bam.bai"
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test3_single_end_markduplicates_sorted_bam = "${test_data_dir}/genomics/homo_sapiens/illumina/bam/test3.single_end.markduplicates.sorted.bam"
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test3_single_end_markduplicates_sorted_bam = "${test_data_dir}/genomics/homo_sapiens/illumina/bam/test3.single_end.markduplicates.sorted.bam"
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read_group_settings_txt = "${test_data_dir}/genomics/homo_sapiens/illumina/bam/read_group_settings.txt"
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test_paired_end_sorted_cram = "${test_data_dir}/genomics/homo_sapiens/illumina/cram/test.paired_end.sorted.cram"
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test_paired_end_sorted_cram_crai = "${test_data_dir}/genomics/homo_sapiens/illumina/cram/test.paired_end.sorted.cram.crai"
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15
tests/modules/atlas/splitmerge/main.nf
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15
tests/modules/atlas/splitmerge/main.nf
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#!/usr/bin/env nextflow
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nextflow.enable.dsl = 2
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include { ATLAS_SPLITMERGE } from '../../../../modules/atlas/splitmerge/main.nf'
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//MAIN
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workflow test_atlas_splitmerge {
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meta = [ id:'test', single_end:false ]
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bam = file(params.test_data['homo_sapiens']['illumina']['test_paired_end_sorted_bam'], checkIfExists: true)
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bai = file(params.test_data['homo_sapiens']['illumina']['test_paired_end_sorted_bam_bai'], checkIfExists: true)
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settings = file(params.test_data['homo_sapiens']['illumina']['read_group_settings_txt'], checkIfExists: true)
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ATLAS_SPLITMERGE ( [meta, bam, bai, settings, []] )
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}
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5
tests/modules/atlas/splitmerge/nextflow.config
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5
tests/modules/atlas/splitmerge/nextflow.config
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process {
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withName: ATLAS_SPLITMERGE {
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publishDir = { "${params.outdir}/${task.process.tokenize(':')[-1].tokenize('_')[0].toLowerCase()}" }
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}
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}
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11
tests/modules/atlas/splitmerge/test.yml
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11
tests/modules/atlas/splitmerge/test.yml
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- name: atlas splitmerge test_atlas_splitmerge
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command: nextflow run tests/modules/atlas/splitmerge -entry test_atlas_splitmerge -c tests/config/nextflow.config
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tags:
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- atlas
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- atlas/splitmerge
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files:
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- path: output/atlas/test.paired_end.sorted_ignoredReads.txt.gz
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md5sum: 9b64c47313d2de89c26790f713707ee6
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- path: output/atlas/test.paired_end.sorted_mergedReads.bam
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- path: output/atlas/versions.yml
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md5sum: 11735bec9c2f4b395b987fd00d4e4294
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